Canonical Allele Identifier: CA2670598941
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52028700-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028700C>T , CM000666.2:g.52028700C>T GRCh38
NC_000004.11:g.52894866C>T , CM000666.1:g.52894866C>T GRCh37
NC_000004.10:g.52589623C>T NCBI36
NG_008891.1:g.14620G>A , LRG_204:g.14620G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.621+30G>A MANE Select ENSP00000370839.6:n.621+30G>A
ENST00000381431.9:c.621+30G>A ENSP00000370839.5:n.621+30G>A
NM_000232.4:c.621+30G>A , LRG_204t1:c.621+30G>A NP_000223.1:n.621+30G>A
XM_006714049.2:c.324+30G>A XP_006714112.1:n.324+30G>A
XM_011534403.1:c.411+30G>A XP_011532705.1:n.411+30G>A
XM_011534404.1:c.324+30G>A XP_011532706.1:n.324+30G>A
NM_000232.5:c.621+30G>A MANE Select NP_000223.1:n.621+30G>A
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